Orantech
- Primary DI
- 06941691975151
- Brand
- Orantech
- Company
- Orantech Inc.
- Model
- BPH-NS30-059Z-60
- Device description
- Philips Compatible, Infant/Neonate, Single tube, 3.0m
- Published
- 2023-10-10
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| DXQ | Blood Pressure Cuff |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| DXQ | Blood Pressure Cuff | Cardiovascular | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 06941691975151 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 06941691975151 | 06941691975151 | 6941691975151 |
GMDN Terms
| Term | Definition |
|---|
| External cuff/pad connection tubing | A length of flexible tube intended to be used to deliver air and/or fluid from a pump to a noninvasive, patient-contact pad, pack or cuff. It may be intended for use with a specific type of assembly (e.g., circulating-air/fluid thermal therapy system, electronic sphygmomanometer, venous compression system). It is typically made of synthetic material and may be intended to be permanently attached to the system control unit. This is a reusable device. |
Regulatory Flags
- DUNS number
- 544423370
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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